Abstract:
:Tools for conducting high-throughput kinome analysis do not exist for many species. For example, two commonly used techniques for monitoring phosphorylation events are phosphorylation-specific antibodies and peptide arrays. The majority of phosphorylation-specific antibodies are for human or mouse targets, and the construction of peptide arrays relies on information from phosphorylation databases, which are similarly biased toward human and mouse data. This is a substantial obstacle because many species other than mouse represent important biological models. On the basis of the observation that phosphorylation events are often conserved across species with respect to their relative positioning within proteins and their biological function, we demonstrate that it is possible to predict the sequence contexts of phosphorylation events in other species for the production of peptide arrays for kinome analysis. Through this approach, genomic information can be rapidly used to create inexpensive, customizable, species-specific peptide arrays for high-throughput kinome analysis. We anticipate that these arrays will be valuable for investigating the conservation of biological responses across species, validating animal models of disease, and translating research to clinical applications.
journal_name
Sci Signaljournal_title
Science signalingauthors
Jalal S,Arsenault R,Potter AA,Babiuk LA,Griebel PJ,Napper Sdoi
10.1126/scisignal.254pl1subject
Has Abstractpub_date
2009-01-20 00:00:00pages
pl1issue
54eissn
1945-0877issn
1937-9145pii
scisignal.254pl1journal_volume
2pub_type
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